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7-Azabicyclo[4.1.0]heptane, 7-(phenylsulfonyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

81097-47-4

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81097-47-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 81097-47-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,1,0,9 and 7 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 81097-47:
(7*8)+(6*1)+(5*0)+(4*9)+(3*7)+(2*4)+(1*7)=134
134 % 10 = 4
So 81097-47-4 is a valid CAS Registry Number.

81097-47-4SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name N-benzenesulfonyl-7-azabicyclo[4.1.0]heptane

1.2 Other means of identification

Product number -
Other names 7-(benzenesulfonyl)-7-azabicyclo[4.1.0]heptane

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:81097-47-4 SDS

81097-47-4Relevant academic research and scientific papers

Base-promoted elaboration of aziridines

Mordini, Alessandro,Russo, Francesco,Valacchi, Michela,Zani, Lorenzo,Degl'Innocenti, Alessandro,Reginato, Gianna

, p. 7153 - 7163 (2007/10/03)

The base-promoted isomerization of aziridines to allyl amines is still an almost unknown reaction. However, the use of superbasic reagents has shown to be able to promote a regio- and stereoselective conversion of monocyclic and bicyclic sulfonyl aziridin

Palladium-Catalyzed Cyclization of ω-Olefinic Tosamides. Synthesis of Nonaromatic Nitrogen Heterocycles

Hegedus, Louis S.,McKearin, James M.

, p. 2444 - 2451 (2007/10/02)

The cyclization of aliphatic amino olefins to nonaromatic nitrogen heterocycles nas been accomplished by conversion of the amine to the corresponding p-toluenesulfonamide, followed by Pd(II)-catalyzed intramolecular amination of the olefin.The resulting t

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